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Thiazole, 5-ethyl-2-phenyl-

Base Information Edit
  • Chemical Name:Thiazole, 5-ethyl-2-phenyl-
  • CAS No.:10045-49-5
  • Molecular Formula:C11H11NS
  • Molecular Weight:189.281
  • Hs Code.:
  • DSSTox Substance ID:DTXSID701313405
  • Nikkaji Number:J144.004G
  • Mol file:10045-49-5.mol
Thiazole, 5-ethyl-2-phenyl-

Synonyms:Thiazole, 5-ethyl-2-phenyl-;5-Ethyl-2-phenyl-1,3-thiazole;5-Ethyl-2-phenylthiazole;10045-49-5;SCHEMBL153089;DTXSID701313405;5-Ethyl-2-phenyl-1,3-thiazole #

Suppliers and Price of Thiazole, 5-ethyl-2-phenyl-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 3 raw suppliers
Chemical Property of Thiazole, 5-ethyl-2-phenyl- Edit
Chemical Property:
  • Boiling Point:172 °C (22 mmHg) 
  • PSA:41.13000 
  • LogP:3.37250 
  • XLogP3:3.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:189.06122053
  • Heavy Atom Count:13
  • Complexity:154
Purity/Quality:

98%,99%, *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCC1=CN=C(S1)C2=CC=CC=C2
Technology Process of Thiazole, 5-ethyl-2-phenyl-

There total 2 articles about Thiazole, 5-ethyl-2-phenyl- which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In toluene; at 130 ℃; for 3h;
DOI:10.1039/d1nj04047b
Guidance literature:
Erhitzen von /BRN= 976106/ mit HI in Ggw. von P;
Guidance literature:
With bromine; In chloroform; acetonitrile; at 0 - 20 ℃;
DOI:10.1039/d1nj04047b
upstream raw materials:

2-bromobutanal

benzenecarbothioamide

Downstream raw materials:

5-ethyl-2-(4-nitro-phenyl)-thiazole

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